Single Peptide Backbone Surrogate Mutations to Regulate Angiotensin GPCR Subtype Selectivity. Issue 47 (21st July 2020)

• Record Type: Journal Article
• Authors: Vrettos, Eirinaios I.; Valverde, Ibai E.; Mascarin, Alba; Pallier, Patrick N.; Cerofolini, Linda; Fragai, Marco; Parigi, Giacomo; Hirmiz, Baydaa; Bekas, Nick; Grob, Nathalie M.; Stylos, Evgenios Κ.; Shaye, Hamidreza; Del Borgo, Mark; Aguilar, Marie‐Isabel; Magnani, Francesca; Syed, Nelofer; Crook, Timothy; Waqif, Emal; Ghazaly, Essam; Cherezov, Vadim; Widdop, Robert E.; Luchinat, Claudio; Michael‐Titus, Adina T.; Mindt, Thomas L.; Tzakos, Andreas G.
• Is Part Of: Chemistry. Volume 26:Issue 47(2020)
• Page Start: 10690
• Page End: 10694
• Publication Date: 2020-07-21
• Subjects: click chemistry -- competition-binding experiments -- G-protein-coupled receptors -- neurotrophic effects -- peptidomimetics; Chemistry -- Periodicals; 540
• DOI: 10.1002/chem.202000924
• Languages: English
• ISSNs: 0947-6539

Abstract

Abstract: Mutating the side‐chains of amino acids in a peptide ligand, with unnatural amino acids, aiming to mitigate its short half‐life is an established approach. However, it is hypothesized that mutating specific backbone peptide bonds with bioisosters can be exploited not only to enhance the proteolytic stability of parent peptides, but also to tune its receptor subtype selectivity. Towards this end, four [Y] 6 ‐Angiotensin II analogues are synthesized where amide bonds have been replaced by 1, 4‐disubstituted 1, 2, 3‐triazole isosteres in four different backbone locations. All the analogues possessed enhanced stability in human plasma in comparison with the parent peptide, whereas only two of them achieved enhanced AT2 R/AT1 R subtype selectivity. This diversification has been studied through 2D NMR spectroscopy and unveiled a putative more structured microenvironment for the two selective ligands accompanied with increased number of NOE cross‐peaks. The most potent analogue, compound 2, has been explored regarding its neurotrophic potential and resulted in an enhanced neurite growth with respect to the established agent C21. Abstract : Through backbone amide bond substitutions with 1, 4‐disubstituted 1, 2, 3‐triazole rings in strategic positions, the proteolytic stability in human plasma is enhanced and simultaneously the AT2 R/AT1 R G‐protein‐coupled receptor (GPCR) subtype selectivity is tuned while retaining the neurotrophic effects of peptide ligands derived from [Y] 6 ‐Angiotensin II.